Comparison of Erector Spinae Plane Block and Caudal Block for Postoperative Analgesia in Pediatric Patients Undergoing Orchiopexy
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 84
- 试验地点
- 1
- 主要终点
- Time To First Analgesic Requirement After Surgery
研究概览
简要总结
This study aims to compare the analgesic efficacy of ultrasound-guided erector spinae plane block and caudal block for postoperative pain management in pediatric patients undergoing orchiopexy. Postoperative pain scores, time to first rescue analgesic requirement, total analgesic consumption, and block-related adverse effects will be evaluated during the first 24 hours after surgery. The study will assess whether erector spinae plane block provides effective postoperative analgesia comparable to or superior to caudal block in pediatric orchiopexy.
研究设计
- 研究类型
- Observational
- 观察模型
- Other
- 时间视角
- Prospective
入排标准
- 年龄范围
- 1 Year 至 7 Years（Child）
- 性别
- Male
- 接受健康志愿者
- 是
入选标准
- •Children aged 1 to 7 years with ASA physical status I-II undergoing unilateral orchiopexy surgery.
排除标准
- •ASA physical status ≥ III
- •History of prematurity (gestational age < 37 weeks) Known coagulation disorders or bleeding tendency
- •Infection, inflammation, or skin lesion at the injection site
- •Known neurological or neuromuscular diseases
- •Presence of significant cardiac or pulmonary disease (e.g., congenital heart disease, active asthma)
- •Hepatic or renal dysfunction
- •Known allergy or hypersensitivity to local anesthetics (e.g., bupivacaine, lidocaine)
- •Developmental delay or cognitive impairment that prevents accurate pain assessment
- •Use of additional regional analgesia techniques (e.g., caudal block) during surgery
- •Block failure or intraoperative complications requiring exclusion from protocol analysis
- •Lack of parental consent for participation in the study
研究组 & 干预措施
Children aged 1-7 years undergoing orchiopexy who received a sacral erector spinae plane block
Children aged 1-7 years undergoing orchiopexy who received a sacral erector spinae plane block
Children aged 1-7 years undergoing orchiopexy who received a caudal block
Children aged 1-7 years undergoing orchiopexy who received a caudal block
结局指标
主要结局
Time To First Analgesic Requirement After Surgery
时间窗: First 24 hours postoperatively
The time elapsed from the end of surgery to the administration of the first rescue analgesic
次要结局
- FLACC Pain Scores at Specified Time Intervals(first 24 hours postoperatively)
研究者
Kübra Demir
resident doctor
Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization